Abstract

Whole genome analysis was performed on 501 isolates obtained from a previous survey which recovered 139 positive environmental sponge samples (i.e., up to 4 isolates per sample) from a total of 719 samples collected at 40 standardized sites in 3 commercial apple packinghouse facilities (i.e., P1, P2, and P3) over 3 successive seasons in a single production year. After excluding duplicated isolates, the data from 156 isolates revealed the clonal diversity of L. monocytogenes and allowed the detection of transient contamination, persistent contamination, and cross-area transmission events. Facility P2 with the poorest sanitary conditions had the least diversity (Shannon’s index of 0.38). P2 contained a Clonal Complex (CC) 554, serogroup IVb-v1 strain that persisted throughout the year and spread across the entire facility, a singleton Sequence Type (ST) 1003, lineage III strain that persisted through two seasons and spread across two areas of the facility, and 3 other clones from transient contaminations. P1 and P3, facilities with better sanitary conditions, had much higher diversity (i.e., 15 clones with a Shannon’s index of 2.49 and 10 clones with a Shannon’s index of 2.10, respectively) that were the result of transient contamination. Facilities P1 and P3 had the highest incidence (43.1%) of lineage III isolates, followed by lineage I (31.3%) and lineage II (25.5%) isolates. Only 1 isolate in the three facilities contained a premature stop codon in virulence gene inlA. Fourteen samples yielded 2–3 clones per sample, demonstrating the importance of choosing appropriate methodologies and selecting a sufficient number of isolates per sample for studying L. monocytogenes diversity. Only 1 isolate, belonging to CC5 and from facility P3, contained a known plasmid, and this was also the only isolate containing benzalkonium chloride tolerance genes. The persistent CC554 strain did not exhibit stronger sanitizer resistance than other isolates and did not contain any confirmed molecular determinants of L. monocytogenes stress resistance that were differentially present in other isolates, such as genes involved in sanitizer tolerance, heavy metal resistance, biofilm-forming, stress survival islet 1 (SSI-1), stress survival islet 2 (SSI-2) or Listeria genomic island (LGI2).

Highlights

  • Listeria monocytogenes is estimated to cause over 1,600 illnesses and 250 deaths annually in the United States, making it one of the leading causes of death from foodborne illness (Silk et al, 2012)

  • High resolution of WGS analysis of L. monocytogenes from 3 apple packinghouses collected in 1 year revealed the clonal diversity of L. monocytogenes and allowed the detection of transient contamination, persistent contamination, and cross-area transmission events

  • The facility P2, with the poorest sanitary conditions, had the least diversity of L. monocytogenes clones; P2 contained a CC554, serogroup IVb-v1 strain persisting through the year and spreading across entire facility, an ST1003, lineage III strain persisting through two seasons and spreading across two areas of the facility, and several other strains due to transient contaminations

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Summary

Introduction

Listeria monocytogenes is estimated to cause over 1,600 illnesses and 250 deaths annually in the United States, making it one of the leading causes of death from foodborne illness (Silk et al, 2012). Persons with immunocompromising conditions, and pregnant women and their newborns are at higher risk of listeriosis than the general population (Silk et al, 2012). The relatively large size of this outbreak (35 cases in 7 states) suggests persistence or repeated contamination of L. monocytogenes that allowed contamination of whole apples used to make caramel apples. Fresh produce is a well-established source of listeriosis, apples were an unexpected vehicle, given their high acidity that generally does not support L. monocytogenes growth. L. monocytogenes have been shown to survive for extended periods of time on experimentally contaminated Red Delicious, Fuji and Granny Smith apples and that the common practice of waxing could facilitate long-term survival of L. monocytogenes on apples (Macarisin et al, 2019)

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